Remote Associate Director, Pharmacovigilance Leader

Pharmaron Beijing Co. Ltd.; United States; Remote; USD 180,000 - 240,000; Full time

Benefits offered by this job

Medical, Dental & Vision Insurance

401(k) with employer matching

PTO and company holidays

HSA contributions

Job summary

Pharmaron is seeking an Associate Director, Pharmacovigilance to establish and lead its U.S. pharmacovigilance operations. As the first dedicated PV hire in the United States, you will shape the future of our U.S.

drug safety services, set up processes, and build a U.S.-based PV team while collaborating with global teams. You will independently manage PV projects, lead client discussions, develop safety plans, and ensure compliance with FDA requirements and ICH guidance in a growing CRO

Qualifications

• Bachelor's degree or higher in Pharmacy, Medicine, Nursing, Life Sciences, or related discipline.
• At least 8 years of progressive experience in pharmacovigilance or drug safety with clinical development exposure.
• Strong knowledge of FDA pharmacovigilance regulations, ICH guidance, and global safety reporting requirements.

Responsibilities

• Establish and lead U.S. pharmacovigilance operations and SOPs.
• Manage client relationships and PV programs with cross-functional teams.
• Oversee safety surveillance, ICSR processing, and regulatory reporting.
• Support business growth and continuous improvement of PV services.

Skills

Pharmacovigilance

FDA regulations

Project management

Client communication

Education

Bachelor's degree in Life Sciences

Tools

PV databases

Safety reporting tools

Job description

Pharmaron is seeking an Associate Director, Pharmacovigilance to establish and lead its U.S. pharmacovigilance operations. As the first dedicated PV hire in the United States, you will shape the future of our U.S.

drug safety services, set up processes, and build a U.S.-based PV team while collaborating with global teams. You will independently manage PV projects, lead client discussions, develop safety plans, and ensure compliance with FDA requirements and ICH guidance in a growing CRO